Purpose of the Analysis
- Identify inherited mutations in BRCA1 and BRCA2 genes
- Assess lifetime risk for breast, ovarian, and prostate cancers
- Guide family members toward preventive screening if a mutation is found
Book BRCA1 & BRCA2 Genetic Test | Lahalak Medical Platform
This advanced genetic screening identifies mutations in BRCA1 and BRCA2 genes, providing essential insights into hereditary cancer risks. Empower yourself with knowledge for early detection and proactive preventive healthcare strategies.
Scientific name: Comprehensive BRCA1 and BRCA2 Mutation Analysis
An advanced genetic test involving full DNA sequencing and deletion/duplication analysis of BRCA1 and BRCA2 genes to accurately assess hereditary cancer risks and guide personalized preventive care.
Service type
Genetic laboratory test
Duration
15-20 minutes
Fasting
Fasting is not required
Included Services
- Sample collection (Blood or Saliva)
- Full gene sequencing
- Deletion/Duplication analysis (MLPA)
- Detailed medical report
Medical Service Information
Who Should Get Tested?
- Individuals with a strong family history of breast or ovarian cancer
- Patients diagnosed with breast cancer at age 50 or younger
- Those with relatives known to have a BRCA gene mutation
Understanding Results
- Positive Result: A mutation was found that increases cancer risk, requiring medical surveillance
- Negative Result: No known mutation was found, though general risk still exists
- Variant of Uncertain Significance: A genetic change was found with unknown health effects
Conditions & Notices
- Genetic counseling is recommended before testing
- Results are not affected by medications or current health status
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